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IDO
T11614 IDO-IN-11 IDO-IN-11 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.18 μM (Kinase) and 0.014 μM (Hela Cell).
T11615 IDO-IN-12 IDO-IN-12 is an indoleamine 2,3-dioxygenase (IDO) inhibitor.
T11617 IDO-IN-3 IDO-IN-3 is a potent indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 290 nM).
T11619 IDO-IN-5 IDO-IN-5 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM).
T11620 IDO-IN-6 IDO-IN-6 is an indoleamine 2,3-dioxygenase (IDO) inhibitor.
T11621 IDO-IN-8 IDO-IN-8  is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM).
T11622 IDO-IN-9 IDO-IN-9 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.011 μM (Kinase) and 0.0018 μM (Hela Cell).
T11624 IDO1-IN-2 IDO1-IN-2 is a potent and selective IDO1 inhibitor with IC50s of 81 nM, 59 nM (mouse), and 28 nM (rat), respectively. It has anti-cancer activity.
T11626 IACS-8968 IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
T11627 IACS-8968 R-enantiomer IACS-8968 R-enantiomer is the R-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
T11628 IACS-8968 S-enantiomer IACS-8968 S-enantiomer is the S-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
T11901 IDO1-IN-5 IDO1-IN-5 is a selective, potent and brain penetrated inhibitor of IDO1 activity, binds to apo-IDO1 lacking heme rather than mature heme-bound IDO1.
T1806 NLG919 NLG919 is a potent IDO (indoleamine-(2, 3)-dioxygenase) pathway inhibitor.
T20513 IDO1-IN-1 IDO1-IN-1 is an indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor.
T2647 INCB024360 analogue IDO-IN-2 is an effective IDO1 inhibitor(IC50=10 nM).
T3548 Epacadostat Epacadostat is an oral-available inhibitor of indoleamine 2, 3-dioxygenase (IDO1), increasing the proliferation and activation of various immune cells and reducing tumor-associated
T4142 DO-IN-2 IDO-IN-2 is an IDO inhibitor extracted from patent WO/2015031295 A1, compound example 1.
T4307 PF06840003 PF-06840003 is a specific and oral active IDO-1 inhibitor.
T4532 Linrodostat BMS-986205 is a selective indoleamine 2, 3-dioxygenase 1 (IDO1) inhibitor.
T5S0053 Coptisine 1. Coptisine treatment increases cell viability based on its reversal effect on the enhanced activity of Indoleamine 2, 3-dioxygenase . 2. Coptisine treats myocardial I/R likely th
T5S0056 Coptisine chloride 1. Coptisine chloride can be absorbed across intestinal epithelial cells, and completely absorbed compounds.
T6407 Beta-Lapachone Beta-Lapachone is a specific DNA topoisomerase I inhibitor, and no inhibitory activities against DNA topoisomerase II or ligase.
T6543 Indoximod Indoximod is a methylated tryptophan with immune checkpoint inhibitory activity. Indoximod inhibits the enzyme indoleamine 2, 3-dioxygenase (IDO), which degrades the essential amin
T8214 Flemiphilippinin D Kushenol E is a class of flavonoids isolated from Sophora flavescens. It is a non-competitive IDO1 inhibitor (IC50: 7.7 µM, Ki: 9.5 µM), has anti-tumor activity.
TQ0071 Navoximod Navoximod (NLG-​919, GDC-0919) is a potent indoleamine-(2,3)-dioxygenase (IDO) pathway inhibitor (Ki/EC50: 7 nM/75 nM).
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